Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Neuromuscular Diseases

Synonyms

Fasciculation Cramp Syndrome, Benign

Definitions

A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA.

ID

http://purl.bioontology.org/ontology/MESH/D009468

altLabel

Fasciculation Cramp Syndrome, Benign

Amyotonia Congenita

Syndrome, Foley-Denny-Brown

Cramp-Fasciculation Syndromes

Foley-Denny-Brown Syndrome

Syndrome, Cramp-Fasciculation

Benign Fasciculation-Cramp Syndromes

Cramp-Fasciculation Syndrome

Fasciculation-Cramp Syndromes, Benign

Foley Denny Brown Syndrome

Neuromuscular Disease

Oppenheim's Disease

Fasciculation-Cramp Syndrome, Benign

Syndromes, Cramp-Fasciculation

Cramp Fasciculation Syndrome

Oppenheim Disease

Oppenheims Disease

Benign Fasciculation-Cramp Syndrome

AN

GEN; do not confuse xref AMYOTONIA CONGENITA with MYOTONIA CONGENITA

AQL

BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C0027868

C0002735

C0751381

DC

1

definition

A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA.

DX

19710101

HN

1971; AMYOTONIA CONGENITA was heading 1963-96

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D021081

http://purl.bioontology.org/ontology/MESH/D003389

http://purl.bioontology.org/ontology/MESH/D020274

http://purl.bioontology.org/ontology/MESH/D020196

http://purl.bioontology.org/ontology/MESH/D009461

http://purl.bioontology.org/ontology/MESH/D009421

http://purl.bioontology.org/ontology/MESH/D020752

http://purl.bioontology.org/ontology/MESH/D003711

http://purl.bioontology.org/ontology/MESH/D012893

http://purl.bioontology.org/ontology/MESH/D002493

http://purl.bioontology.org/ontology/MESH/D012148

http://purl.bioontology.org/ontology/MESH/D020258

http://purl.bioontology.org/ontology/MESH/D009423

http://purl.bioontology.org/ontology/MESH/D019636

http://purl.bioontology.org/ontology/MESH/D001342

Machine permutation

1971; AMYOTONIA CONGENITA was heading 1963-96; for MYATONIA CONGENITA & OPPENHEIM'S DISEASE see AMYOTONIA CONGENITA 1963-1996

Mapped from

http://purl.bioontology.org/ontology/MESH/C565542

http://purl.bioontology.org/ontology/MESH/C536229

http://purl.bioontology.org/ontology/MESH/C000629404

http://purl.bioontology.org/ontology/MESH/C565544

http://purl.bioontology.org/ontology/MESH/C565543

http://purl.bioontology.org/ontology/MESH/C565541

http://purl.bioontology.org/ontology/MESH/C564022

MDA

19990101

MMR

20120703

MN

C10.668

notation

D009468

prefLabel

Neuromuscular Diseases

TERMUI

T373390

T028217

T028218

T373389

T028214

T373391

T028216

TH

NLM (1971)

NLM (2000)

NLM (1997)

OMIM (2013)

tui

T019

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D009422

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http://purl.bioontology.org/ontology/MEDLINEPLUS/C0027868 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/ICD10CM/G70.9 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/205000 Online Mendelian Inheritance in Man CUI
http://purl.bmicc.cn/ontology/ICD10CN/G70.9 International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/ICD10/G70.9 International Classification of Diseases, Version 10 CUI